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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030906Generated: October 31, 2026

Potassium Carbonate → ethyl 4-[3-[4-(5,6-dihydro-4H-1,3-oxazin-2-yl)phenoxy]propyl]-1-piperidinecarboxylate

https://huagongshe.com/reaction/1030906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-(3-chloropropyl)-1-piperidinecarboxylateHCID 14989201—
Reactant4-(5,6-dihydro-4H-1,3-oxazin-2-yl)phenol hydrochlorideHCID 136404538—
SolventDimethylformamideHCID 6228—
Productethyl 4-[3-[4-(5,6-dihydro-4H-1,3-oxazin-2-yl)phenoxy]propyl]-1-piperidinecarboxylateHCID 1498920371.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 15 parts of 4-(5,6-dihydro-4H-1,3-oxazin-2-yl)phenol hydrochloride, 29 parts of potassium carbonate and 180 parts of N,N-dimethylformamide was stirred for 1 hour at about 80° C. Then there were added 16.4 parts of ethyl 4-(3-chloropropyl)-1-piperidinecarboxylate and stirring was continued overnight at about 95° C. The reaction mixture was poured into ice water and the product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (98.5:1.5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 18.8 parts (71.7%) of ethyl 4-[3-[4-(5,6-dihydro-4H-1,3-oxazin-2-yl)phenoxy]propyl]-1-piperidinecarboxylate; mp. 128.5° C. (int. 59).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106973
Source datasetuspto-grants-1992_04
ORD IDord-c36a8691f6404a01b0cbfc73e18beca3
Source noteuspto-grants-1992_04